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Green synthesis of chicory (Cichorium intybus L.) Chitosan nanoparticles and evaluation of their anti-fungal, anti-hemolytic, and anti-cancer activities 菊苣的绿色合成壳聚糖纳米颗粒及其抗真菌、抗溶血和抗癌活性的评价
IF 1.7 4区 生物学 Q3 Materials Science Pub Date : 2022-10-13 DOI: 10.1177/08839115221126737
M. Tuorkey, Y. Khedr, Samar M Aborhyem, Xiang Xue
Chicory (Cichorium intybus L.) is widely consumed as a food plant in many regions of the world and has been involved in traditional medicine due to its unique contents of phytochemicals. We aimed to investigate the anti-fungal, anti-hemolytic, and anti-cancer activities of chicory roots and leaves ethanolic extracts, and their Chitosan nanoparticles (Chit NPs) formulations. The ethanolic extract of chicory roots and leaves were microencapsulated into Chit NPs. The anti-hemolytic, anti-fungal, and anti-cancer activity of chicory extracts and their Chit-NPs were investigated, along with an in vitro toxicological study. Chicory extracts encapsulation into Chit NPs increased their anti-fungal activity against two fungal pathogens, Candida albicans and Aspergillus flavus. Chicory extracts and their Chit NPs appeared strong anti-hemolytic activity in hypotonic media. Due to microencapsulation of roots and leaves extracts into Chit NPs, the IC50 was decreased 2.49 and 2.6-folds in HepG2 and MCF-7 cell lines, and 6.31 and 5.50-folds in HepG2 and MCF-7 cell lines, respectively. The in vitro toxicological study revealed that the IC50 of chicory roots (56.84 ± 6.4 μg/ml) and leaves (45.51 ± 4.2 μg/ml) decreased 8.45 and 6.77-folds in the normal human fibroblasts (WI38) cell line, compared to Doxorubicin (6.72 ± 0.5 μg/ml). Microencapsulation of extracts into Chit NPs increased their toxicity 2.43-folds for Chit-Roots NPs (IC50 = 23.35 ± 2.3 μg/ml) and 1.22-fold for Chit-Leaves NPs (IC50 = 37.29 ± 2.9 μg/ml). Chicory-Chit NPs possess promising anti-cancer and anti-hemolytic activities. It is worth for further testing their efficacy and toxicity in pre-clinical animal models as well as clinical trials.
菊苣(chicicorium intybus L.)是世界上许多地区广泛食用的一种食用植物,由于其独特的植物化学成分,已被用于传统医学。研究菊苣根、叶乙醇提取物及其壳聚糖纳米颗粒(Chit NPs)的抗真菌、抗溶血和抗癌活性。将菊苣根和菊苣叶的乙醇提取物微囊化成Chit NPs。研究了菊苣提取物及其Chit-NPs的抗溶血、抗真菌和抗癌活性,并进行了体外毒理学研究。菊苣提取物包埋在Chit NPs中,对白色念珠菌和黄曲霉的抗真菌活性增强。菊苣提取物及其Chit NPs在低渗介质中表现出较强的抗溶血活性。根和叶提取物被微胶囊化后,HepG2和MCF-7细胞株的IC50分别降低了2.49倍和2.6倍,HepG2和MCF-7细胞株的IC50分别降低了6.31倍和5.50倍。体外毒理学研究表明,菊苣根(56.84±6.4 μg/ml)和叶片(45.51±4.2 μg/ml)对正常人成纤维细胞(WI38)的IC50比阿霉素(6.72±0.5 μg/ml)分别降低8.45倍和6.77倍。将提取物微胶囊化后,其对甜菜根NPs的毒性提高2.43倍(IC50 = 23.35±2.3 μg/ml),对甜菜叶NPs的毒性提高1.22倍(IC50 = 37.29±2.9 μg/ml)。菊苣NPs具有良好的抗癌和抗溶血活性。值得在临床前动物模型和临床试验中进一步验证其有效性和毒性。
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引用次数: 3
Effect of pH on salicylic acid-based poly(anhydride-ester): Implications for polymer degradation and controlled salicylic acid release pH对水杨酸基聚酸酐酯的影响:对聚合物降解和控制水杨酸释放的影响
IF 1.7 4区 生物学 Q3 Materials Science Pub Date : 2022-09-28 DOI: 10.1177/08839115221121844
Sammy Gulrajani, S. Snyder, Jason D. Hackenberg, K. Uhrich
Salicylic acid (SA)-based poly(anhydride-esters) (SAPAEs) hydrolytically degrade to release SA in a controlled manner over extended time periods. While these polymers have been well investigated under in vivo conditions, this study is the first detailed, systematic assessment of in vitro polymer degradation over a range of pH values. To investigate the effect of pH conditions on SAPAE degradation, in vitro degradation studies were conducted on SAPAE disks over a wide pH range (2.0, 4.0, 6.0, 7.4, 8.0, 9.0, and 10.0) for 30 days. Several parameters were evaluated, including SA concentrations in the degradation media, polymer mass loss, water uptake in the polymer matrices, and SA solubility at different pH values to substantiate SA release results and characterize the in vitro polymer degradation process. Complete SA release was achieved at more basic conditions (pH 9.0 and 10.0) over 9 days, whereas less than 41% SA was released over the same time period at neutral pH conditions (pH 8.0 and 7.4). By comparison, SA release was minimal in acidic pH conditions. Overall, we present quantitative data of polymer degradation as defined by SA in vitro release, which increased with increasing pH values. More basic conditions promoted polymer degradation, whereas acidic conditions minimized polymer degradation.
水杨酸(SA)为基础的聚酸酐酯(sapae)水解降解释放SA在一段时间内可控的方式。虽然这些聚合物已经在体内条件下进行了很好的研究,但本研究是第一次详细、系统地评估体外聚合物在一定pH值范围内的降解。为了研究pH条件对SAPAE降解的影响,我们在较宽的pH范围(2.0、4.0、6.0、7.4、8.0、9.0和10.0)下对SAPAE圆盘进行了30天的体外降解研究。研究评估了几个参数,包括降解介质中的SA浓度、聚合物质量损失、聚合物基质中的吸水率和不同pH值下SA的溶解度,以证实SA释放结果并表征体外聚合物降解过程。在碱性条件(pH 9.0和10.0)下,SA在9天内完全释放,而在中性pH条件(pH 8.0和7.4)下,SA在相同时间内的释放量不到41%。相比之下,SA在酸性pH条件下释放最少。总的来说,我们给出了聚合物降解的定量数据,即SA体外释放,随着pH值的增加而增加。更基本的条件促进聚合物降解,而酸性条件最小化聚合物降解。
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引用次数: 2
Upon a potential approach to regulate the targeting region of inhalable liposomes 一种调节可吸入脂质体靶向区域的潜在方法
IF 1.7 4区 生物学 Q3 Materials Science Pub Date : 2022-09-09 DOI: 10.1177/08839115221121862
Lei Shu, Zhengwei Huang, Ying Huang, Chuanbin Wu, Xin Pan
Liposomes for inhalation have high biosafety and can achieve slow and controlled delivery, which are especially suitable for the treatment of lung diseases and have a promising clinical application prospect. However, liposomes for inhalation have the key bottleneck problem of the lack of strategies to control the targeting region, which restricts its clinical transformation. The root cause is the inability to control the bio-corona (BC) generation upon liposomes, which dominates the specific targeting regions. In order to overcome the above bottleneck, a high density hybrid liposome system based on distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)] (DSPE-PEG) may be a potential choice. The PEG chain in DSPE-PEG has “stealth” effect that can hinder the adsorption of biological molecules. When the density of DSPE-PEG hybridization is high, the “stealth” effect is more significant, and the total adsorption amount of liposomal BC can be effectively reduced. By optimizing the PEG chain structures of DSPE-PEG, viz PEG chain length and terminal group modification, DSPE-PEG high density hybrid liposomes can be endowed with the function of targeting site regulation based on BC domination effect. It is believed that this proposed system can promote the profound reform of the research paradigm of inhalational liposomes, and accelerate the development of related products.
吸入用脂质体生物安全性高,可实现缓慢、可控的给药,特别适用于肺部疾病的治疗,具有广阔的临床应用前景。然而,吸入用脂质体的关键瓶颈问题是缺乏对靶向区域的控制策略,制约了其临床转化。根本原因是无法控制脂质体上的生物冠(BC)的产生,脂质体在特定靶向区域占主导地位。为了克服上述瓶颈,基于二硬脂酰- asn -甘油-3-磷酸乙醇胺- n-[甲氧基(聚乙二醇)](DSPE-PEG)的高密度杂化脂质体体系可能是一个潜在的选择。DSPE-PEG中的PEG链具有“隐身”作用,可以阻碍生物分子的吸附。当DSPE-PEG杂交密度较高时,“隐身”效应更为显著,可有效降低脂质体BC的总吸附量。通过对DSPE-PEG的PEG链结构进行优化,即PEG链长和末端基团修饰,使DSPE-PEG高密度杂交脂质体具有基于BC优势效应的靶向位点调控功能。相信该系统能够推动吸入性脂质体研究范式的深刻变革,加速相关产品的开发。
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引用次数: 0
Virucidal properties of new multifunctional fibrous N-halamine-immobilized styrene-divinylbenzene copolymers 新型多功能纤维n -卤胺固定化苯乙烯-二乙烯基苯共聚物的杀病毒性能
IF 1.7 4区 生物学 Q3 Materials Science Pub Date : 2022-09-09 DOI: 10.1177/08839115221121852
B. Murashevych, D. Stepanskyi, V. Toropin, A. Mironenko, H. Maslak, K. Burmistrov, Nataliia Teteriuk
Virucidal properties of N-chlorosulfonamides immobilized on fibrous styrene-divinylbenzene copolymers have been studied. Corresponding materials with different functional group structures and chlorine content have been synthesized on FIBAN polymer carriers in the form of staple fibers and non-woven fabrics. The study has been conducted in general accordance with EN 14476 standard on poliovirus type-1 and adenovirus type-5. It has been found that all tested samples exhibit pronounced virucidal activity: regardless of the carrier polymer form, sodium N-chlorosulfonamides inactivated both viruses in less than 30 s, and N,N-dichlorosulfonamides—in 30–60 s. The main mechanism of action of these materials, obviously, consists in the emission of active chlorine from the functional group into the treated medium under the action of the amino groups of virus fragments and cell culture. Considering the previously described antimicrobial and reparative properties of such materials, as well as their satisfactory physical and mechanical properties, the synthesized polymers are promising for the creation of medical devices with increased resistance to microbial contamination, such as protective masks, filter elements, long-acting wound dressings, and others.
研究了纤维型苯乙烯-二乙烯基苯共聚物固定化n -氯磺酰胺的杀病毒性能。以短纤维和无纺布的形式在FIBAN聚合物载体上合成了具有不同官能团结构和氯含量的相应材料。该研究大体上按照EN 14476关于1型脊髓灰质炎病毒和5型腺病毒的标准进行。研究发现,所有测试样品都表现出明显的杀病毒活性:无论载体聚合物形式如何,N-氯磺胺钠在30秒内灭活了两种病毒,N,N-二氯磺胺在30 - 60秒内灭活了两种病毒。显然,这些物质的主要作用机制是在病毒片段和细胞培养物的氨基的作用下,从官能团向处理培养基中释放活性氯。考虑到上述材料的抗菌和修复性能,以及它们令人满意的物理和机械性能,所合成的聚合物有望用于制造抗微生物污染能力增强的医疗设备,如防护口罩、过滤元件、长效伤口敷料等。
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引用次数: 2
Synthesis of novel chitosan Schiff base and its ZnO nanocomposite for removal of synthetic dye, antimicrobial, and cytotoxicity activity 新型壳聚糖希夫碱及其ZnO纳米复合材料的合成及其对合成染料的去除、抗菌和细胞毒活性
IF 1.7 4区 生物学 Q3 Materials Science Pub Date : 2022-09-01 DOI: 10.1177/08839115221119212
Mostafa M Gaafar, Fathy M Eltaweel, H. A. Fouda, M. Abdelaal
In this work, a novel chitosan Schiff base 4-(2-Hydroxyaniline)pent-3-en-2-one chitosan (2-HyA-CS) and its ZnO nanocomposite (2-HyA-CS/ZnO) were sensitized and characterized by appropriate methods; FTIR, XRD, Elemental analysis, SEM, TEM and TGA. The result of characterization methods confirms the preparation of 2-HyA-CS and 2-HyA-CS/ZnO. The SEM images reveal that chitosan, 2-HyA-CS, and 2-HyA-CS/ZnO have a varied roughness and porous surfaces. The reason for this difference was attributed to the formation of Schiff base 2-HyA-CS and the presence of ZnO nanoparticles in 2-HyA-CS/ZnO. The patterns of XRD and FTIR confirm the formation of 2-HyA-CS and 2-HyA-CS/ZnO. The degree of substitution (DS) of modified chitosan 2-HyA-CS was calculated using Elemental analysis and FTIR.ATR, it was found to be 74%. The adsorption efficiency of the produced adsorbents was compared with pure chitosan to remove of Remazol Brilliant Blue R (RBBR) from an aqueous medium and antimicrobial activity. The removal percentage of RBBR by chitosan, 2-HyA-CS, and 2-HyA-CS/ZnO are 47.12%, 91.9%, and 96.56%, respectively with the following order: 2-HyA-CS/ZnO > 2-HyA-CS > chitosan. Their antimicrobial activities were studied against two Gram negative bacteria (E. coli and P. aeruginosa), two Gram positive bacteria (S. aureus and B. cereus) and (C. albicans) as a yeast strain, the inhibitory zone measurements revealed that the activity of 2-HyA-CS/ZnO is excellent and higher than 2-HyA-CS and pure chitosan. The cytotoxicity of the prepared compound 2-HyA-CS and 2-HyA-CS/ZnO along with pure chitosan was estimated against two human cancer cells MCF-7 cells and HepG-2 cells, the result indicates that 2-HyA-CS/ZnO having higher Inhibitory activity against both MCF-7 and HepG-2 cells with 53.5 ± 2.86 and 27.4 ± 1.23 µg/mL respectively and 2-HyA-CS possessing moderate Inhibitory activity against both MCF-7 and HepG-2 cancer cells with IC50 = 216.5 ± 7.48 and 135.6 ± 6.49 µg/ml respectively.
本文对新型壳聚糖希夫碱- 4-(2-羟基苯胺)-3-烯-2- 1壳聚糖(2-HyA-CS)及其ZnO纳米复合材料(2-HyA-CS/ZnO)进行了敏化和表征;FTIR, XRD,元素分析,SEM, TEM和TGA。表征方法的结果证实了2-HyA-CS和2-HyA-CS/ZnO的制备。SEM图像显示壳聚糖、2-HyA-CS和2-HyA-CS/ZnO具有不同的粗糙度和多孔表面。造成这种差异的原因是席夫碱2-HyA-CS的形成和2-HyA-CS/ZnO中ZnO纳米粒子的存在。XRD和FTIR谱图证实了2-HyA-CS和2-HyA-CS/ZnO的形成。采用元素分析和红外光谱法计算了改性壳聚糖2-HyA-CS的取代度(DS)。ATR为74%比较了所制备的吸附剂与纯壳聚糖对水介质中雷马唑亮蓝R (RBBR)的吸附效率和抗菌活性。壳聚糖、2-HyA-CS和2-HyA-CS/ZnO对RBBR的去除率分别为47.12%、91.9%和96.56%,其去除率依次为:2-HyA-CS/ZnO > 2-HyA-CS >壳聚糖。对两种革兰氏阴性菌(大肠杆菌和铜绿假单胞菌)、两种革兰氏阳性菌(金黄色葡萄球菌和蜡样芽孢杆菌)和酵母菌(白色念珠菌)的抑菌活性进行了研究,抑菌区测定表明,2-HyA-CS/ZnO的抑菌活性优于2-HyA-CS和纯壳聚糖。结果表明,2-HyA-CS/ZnO对MCF-7和HepG-2癌细胞均具有较高的抑制活性,IC50分别为53.5±2.86和27.4±1.23µg/mL; 2-HyA-CS对MCF-7和HepG-2癌细胞均具有中等抑制活性,IC50分别为216.5±7.48和135.6±6.49µg/mL。
{"title":"Synthesis of novel chitosan Schiff base and its ZnO nanocomposite for removal of synthetic dye, antimicrobial, and cytotoxicity activity","authors":"Mostafa M Gaafar, Fathy M Eltaweel, H. A. Fouda, M. Abdelaal","doi":"10.1177/08839115221119212","DOIUrl":"https://doi.org/10.1177/08839115221119212","url":null,"abstract":"In this work, a novel chitosan Schiff base 4-(2-Hydroxyaniline)pent-3-en-2-one chitosan (2-HyA-CS) and its ZnO nanocomposite (2-HyA-CS/ZnO) were sensitized and characterized by appropriate methods; FTIR, XRD, Elemental analysis, SEM, TEM and TGA. The result of characterization methods confirms the preparation of 2-HyA-CS and 2-HyA-CS/ZnO. The SEM images reveal that chitosan, 2-HyA-CS, and 2-HyA-CS/ZnO have a varied roughness and porous surfaces. The reason for this difference was attributed to the formation of Schiff base 2-HyA-CS and the presence of ZnO nanoparticles in 2-HyA-CS/ZnO. The patterns of XRD and FTIR confirm the formation of 2-HyA-CS and 2-HyA-CS/ZnO. The degree of substitution (DS) of modified chitosan 2-HyA-CS was calculated using Elemental analysis and FTIR.ATR, it was found to be 74%. The adsorption efficiency of the produced adsorbents was compared with pure chitosan to remove of Remazol Brilliant Blue R (RBBR) from an aqueous medium and antimicrobial activity. The removal percentage of RBBR by chitosan, 2-HyA-CS, and 2-HyA-CS/ZnO are 47.12%, 91.9%, and 96.56%, respectively with the following order: 2-HyA-CS/ZnO > 2-HyA-CS > chitosan. Their antimicrobial activities were studied against two Gram negative bacteria (E. coli and P. aeruginosa), two Gram positive bacteria (S. aureus and B. cereus) and (C. albicans) as a yeast strain, the inhibitory zone measurements revealed that the activity of 2-HyA-CS/ZnO is excellent and higher than 2-HyA-CS and pure chitosan. The cytotoxicity of the prepared compound 2-HyA-CS and 2-HyA-CS/ZnO along with pure chitosan was estimated against two human cancer cells MCF-7 cells and HepG-2 cells, the result indicates that 2-HyA-CS/ZnO having higher Inhibitory activity against both MCF-7 and HepG-2 cells with 53.5 ± 2.86 and 27.4 ± 1.23 µg/mL respectively and 2-HyA-CS possessing moderate Inhibitory activity against both MCF-7 and HepG-2 cancer cells with IC50 = 216.5 ± 7.48 and 135.6 ± 6.49 µg/ml respectively.","PeriodicalId":15038,"journal":{"name":"Journal of Bioactive and Compatible Polymers","volume":null,"pages":null},"PeriodicalIF":1.7,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76694964","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Influence of gelatin modification on enzymatically-gellable pectin-gelatin hydrogel properties for soft tissue engineering applications 明胶改性对酶凝胶性果胶-明胶水凝胶性能的影响
IF 1.7 4区 生物学 Q3 Materials Science Pub Date : 2022-08-26 DOI: 10.1177/08839115221119210
Asal Ebrahimzadeh, Elnaz Khanalizadeh, Shahla Khodabakhshaghdam, D. Kazemi, Ali Baradar Khoshfetrat
Injectable in situ-forming hydrogels appears to be a promising approach for tissue engineering applications. In this study, the effect of phenol moiety (Ph) addition to gelatin in enzymatically-gellable modified pectin hydrogel (Pec-Ph) was studied. Addition of gelatin-Ph to Pec-Ph (Pec-Ph/Gel-Ph) altered the physical properties of Pec-Ph-based hydrogels as compared to unmodified gelatin (Pec-Ph/Gel) addition. Swelling ratio and degradation rates of the Pec-Ph/Gel-Ph hydrogel decreased 35% and 50%, respectively, and the elasticity of Pec-Ph/Gel-Ph hydrogel was higher than the Pec-Ph/Gel hydrogels. Scanning electron microscopy images showed that the existence of phenolic groups in gelatin decreased the pore size of Pec-Ph/Gel-Ph hydrogels. Culture of chondrocyte cells in the Pec-Ph/Gel-Ph hydrogels showed more metabolic activity (4×) during a 14-day culture period. Hydrogels subcutaneously implanted in rats could also be identified readily without complete absorption and signs of toxicity or any untoward reactions after 1 month. The work showed the potential of Pec-Ph/Gel-Ph hydrogels as a promising in situ injectable hydrogel for soft tissue engineering applications.
可注射的位置形成水凝胶似乎是一个有前途的方法,组织工程应用。本文研究了在酶凝胶改性果胶水凝胶(Pec-Ph)中加入苯酚段(Ph)对明胶性能的影响。与未改性明胶(pecph /Gel)相比,明胶- ph加入到pecph (pecph /Gel)中改变了pecph基水凝胶的物理性质。pecph /Gel- ph水凝胶的溶胀率和降解率分别降低35%和50%,其弹性高于pecph /Gel水凝胶。扫描电镜图像显示,明胶中酚基的存在使peg - ph /Gel-Ph水凝胶的孔径减小。在peg - ph /Gel-Ph水凝胶中培养的软骨细胞在14天的培养期间显示出更高的代谢活性(4倍)。大鼠皮下植入水凝胶,1个月后无完全吸收,无毒性和不良反应迹象。该研究表明,Pec-Ph/Gel-Ph水凝胶是一种有前景的软组织工程原位注射水凝胶。
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引用次数: 0
Study on properties of 3D-printed GelMA hydrogel scaffolds with different nHA contents 不同nHA含量的3d打印凝胶支架性能研究
IF 1.7 4区 生物学 Q3 Materials Science Pub Date : 2022-08-22 DOI: 10.1177/08839115221119211
Yaocheng Wang, Chengxiong Lin
Biological 3D printing is a reliable technology for 3D printing bone repair scaffolds with simple operation, high efficiency, and relatively low cost. Gelatin methacryloyl (GelMA) hydrogels have attracted much attention due to their good biocompatibility, but the poor mechanical properties limit their application in bone reconstruction engineering. In this study, nano-hydroxyapatite (nHA) particles were added to GelMA hydrogels, and the performances of composite hydrogel scaffolds with different nHA contents were investigated in terms of rheological properties, light transmission properties, surface morphology, mechanical properties, and biocompatibility. The experimental results showed that the incorporation of nHA particles could effectively improve the printability and mechanical properties of the scaffolds, the scaffold fibers had better resistance to deformation, improved degradation rate, and biological experiments confirmed that nHA particles had no significant cytotoxicity. However, the addition of HA particles also reduced the light transmission properties of the slurry, and when its content exceeds a certain value, the hydrogel scaffolds show incomplete curing and eventually affect their test performance. The results can offer guidance and reference for the selection of ink and function for 3D printing bone repair scaffold.
生物3D打印是一种可靠的3D打印骨修复支架技术,操作简单,效率高,成本相对较低。明胶甲基丙烯酰(GelMA)水凝胶因其良好的生物相容性而备受关注,但其较差的力学性能限制了其在骨重建工程中的应用。本研究将纳米羟基磷灰石(nHA)颗粒加入到GelMA水凝胶中,从流变性能、透光性、表面形貌、力学性能和生物相容性等方面考察了不同nHA含量的复合水凝胶支架的性能。实验结果表明,nHA颗粒的掺入可以有效提高支架的打印性和力学性能,支架纤维具有更好的抗变形能力,降解率提高,生物实验证实nHA颗粒无明显的细胞毒性。然而,HA颗粒的加入也降低了浆料的透光性能,当其含量超过一定值时,水凝胶支架呈现不完全固化,最终影响其试验性能。研究结果可为3D打印骨修复支架墨水和功能的选择提供指导和参考。
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引用次数: 0
Pullulan and Pluronic F-127 based in situ gel system for intranasal delivery: Development, in vitro and in vivo evaluation 基于Pullulan和Pluronic F-127的鼻腔内给药原位凝胶系统:开发,体外和体内评估
IF 1.7 4区 生物学 Q3 Materials Science Pub Date : 2022-07-07 DOI: 10.1177/08839115221110284
H. Mahajan, V. Jadhao, Sachin M. Chandankar
The current work seeks to use Pullulan and Pluronic F-127 (PF-127), a new gel-forming material, for sildenafil citrate (SLC) intranasal delivery. The cold approach was used to develop an SLC-loaded in situ gel based on thermoreversible polymer PF-127 and mucoadhesive polymer Pullulan. In situ gel systems based on Pullulan responds intelligently to environmental stimuli like charge, pH, temperature, light, and redox. To achieve gelation at physiological temperature formulations were modified to have gelation temperatures lower than 34.1°C. Physical appearance and rheological measurements were used to calculate the temperature of gelation. With the addition of increasing quantities of Pullulan, the gelation temperatures fell (from 34.1°C for 8% w/v, 10% w/v, and 12% w/v 0.5% Pullulan). In the goat nasal mucosal membrane, Pullulan concentration increased the mucoadhesive force in terms of detachment stress. The results of drug permeation testing in vitro investigations over the goat nasal mucosa showed that utilizing an in situ gelling formulation with a Pullulan content of 0.5% or higher can greatly boost the effective penetration coefficient. The formulation was shown to be safe for the nasal mucosa after a histological investigation. Conclusively, Pullulan and PF-127 may be appropriate carriers for SLC intranasal administration.
目前的工作寻求使用Pullulan和Pluronic F-127 (PF-127),一种新的凝胶形成材料,用于枸橼酸西地那非(SLC)的鼻内给药。采用冷法制备了一种基于热可逆聚合物PF-127和黏附聚合物pululan的负载slc的原位凝胶。基于Pullulan的原位凝胶系统对环境刺激(如电荷、pH值、温度、光和氧化还原)做出智能反应。为了在生理温度下实现凝胶化,对配方进行了改性,使凝胶化温度低于34.1℃。物理外观和流变学测量用于计算凝胶温度。随着普鲁兰添加量的增加,凝胶温度下降(8% w/v、10% w/v和12% w/v 0.5%普鲁兰时为34.1℃)。在山羊鼻粘膜中,普鲁兰浓度在剥离应力方面增加了黏附力。体外对山羊鼻黏膜的药物渗透试验结果表明,普鲁兰含量在0.5%以上的原位胶凝制剂可显著提高药物的有效渗透系数。经组织学检查,该制剂对鼻黏膜是安全的。总之,普鲁兰和PF-127可能是鼻内给药SLC的合适载体。
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引用次数: 5
In vivo therapeutic evaluation of a cellulose acetate hydrogel cross linked with ethylenediaminetetraacetic-dianhydride containing propolis ethanolic-extract for treating burns 含有蜂胶乙醇提取物的醋酸纤维素水凝胶与乙二胺四乙酸二酐交联治疗烧伤的体内治疗评价
IF 1.7 4区 生物学 Q3 Materials Science Pub Date : 2022-07-01 DOI: 10.1177/08839115221106869
M. Hausen, A. Melero, J. Asami, L. M. Ferreira, Guilherme Borges Gomes da Silva, Mariana Cesar de Azeredo Bissoli, V. R. Marcato, B. D. Nani, P. Rosalen, S. M. Alencar, V. Botaro, D. Komatsu, A. Senna, E. Duek
An increasing interest in regenerative medicine has been an approach with natural products used for assorted skin treatments. Propolis from Apis mellifera species of bees have shown high acceptance due to antimicrobial and anti-inflammatory properties. However, just a few propolis types presents stronger effects in controlling inflammation. The current work describes an organic propolis recently isolated, named as OP6, that presented strong anti-inflammatory influences in vivo when associated with EDTA cross-linked hydrogel, used as a curative device in second-degree burns in a murine model. We developed a cellulose acetate hydrogel cross-linked with ethylenediaminetetraacetic dianhydride (HAC-EDTA) as a polymeric matrix for a bandage based on an ethanolic extract of propolis at 15%, 30%, and 60% (w/v) for treating second-degree burns. In vivo studies were carried out in Wistar rats divided into three groups: negative control (only lesion), positive control (lesion with HAC-EDTA film), and treatment group (lesion with the HAC-EDTA + OP6 at 15%, 30%, and 60%). Each group was randomized and equally subdivided into two subgroups according to the period of bandage wearing (7 and 14 days). Previous work of this research group selected the propolis OP6 sample source as the best candidate for the in vivo study. HAC-EDTA + OP6 15%, 30%, and 60% films demonstrated a concentration-dependent release rate, with the highest amount of propolis released after tests (484.3 mg) by HAC-EDTA enriched with the highest concentrated extract of propolis. HAC-EDTA + OP6 films were efficient in preventing infections, promoting lesion retraction, and tissue regeneration. The HAC-EDTA + OP6 30% treatment was more efficient, revealing a reduced inflammatory process and stimulating skin regeneration. The designed HAC-EDTA + propolis films were shown as promising tools for second-degree burns treatment, accelerating healing process to a full recovery tissue repair after 14 days.
人们对再生医学越来越感兴趣,这是一种使用天然产品进行各种皮肤治疗的方法。Apis mellifera蜜蜂的蜂胶由于其抗菌和抗炎的特性而被广泛接受。然而,只有少数几种蜂胶在控制炎症方面表现出更强的效果。目前的工作描述了一种最近分离的有机蜂胶,命名为OP6,当与EDTA交联水凝胶结合时,它在体内表现出很强的抗炎作用,在小鼠模型中被用作二度烧伤的治疗装置。我们开发了一种醋酸纤维素水凝胶与乙二胺四乙酸二酐交联(HAC-EDTA)作为聚合物基质,用于基于蜂胶乙醇提取物在15%,30%和60% (w/v)的绷带,用于治疗二度烧伤。Wistar大鼠体内实验分为三组:阴性对照组(仅病变)、阳性对照组(有HAC-EDTA膜的病变)和治疗组(有HAC-EDTA + OP6膜的病变为15%、30%和60%)。各组按绷带佩戴时间(7天和14天)随机分成2个亚组。本课题组前期工作选择蜂胶OP6样品源作为体内研究的最佳候选。15%、30%和60%的HAC-EDTA + OP6膜的释放率呈浓度依赖性,其中浓度最高的蜂胶提取物富集的HAC-EDTA膜的蜂胶释放量最高(484.3 mg)。HAC-EDTA + OP6膜具有有效的预防感染、促进病变回缩和组织再生的作用。30%的HAC-EDTA + OP6治疗更有效,显示炎症过程减少并刺激皮肤再生。设计的HAC-EDTA +蜂胶膜被证明是二度烧伤治疗的有希望的工具,加速愈合过程,在14天后完全恢复组织修复。
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引用次数: 1
Bi-layered PLGA electrospun membrane with occlusive and osteogenic properties for periodontal regeneration 具有封闭和成骨特性的双层聚乳酸静电纺丝膜用于牙周再生
IF 1.7 4区 生物学 Q3 Materials Science Pub Date : 2022-07-01 DOI: 10.1177/08839115221095257
Meiling Zhong, Jixia Lin, Zhimin He, Wuchao Wu, De-hui Ji, Richao Zhang, Jiali Zhang
Guided tissue regeneration (GTR) membranes not only can hamper undesirable tissues down-growth into the defects but also can selectively promote the in-growth of regenerative bone tissue, playing a critical role in periodontal regeneration. Herein, a bi-layered electrospun membrane with different sized pores was designed and fabricated by adjusting electrospinning parameters combing with facile two-step electrospinning. The small-sized pore layer (SL) as occlusive layer consisted of electrospun poly (lactic-co-glycolic acid) (PLGA) nanofibers, while the macroporous osteoconductive layer (ML) was attained via introducing the nano-hydroxyapatite (nHA) particles into PLGA nanofibers during electrospinning. Morphological results such as surface topography, nanofiber size, and pore size distribution, showed that the SL exhibited a dense structure with pore size mainly from 4 to 7 μm. In contrast, the ML possessed a loosely packed structure with pore size mainly from 20 to 28 μm, which was beneficial to the infiltration of the cells. Fourier transform infrared spectroscopy (FTIR), Energy dispersive spectrometer (EDS), and X-ray diffractometry (XRD) results showed that nHA particles were evenly loaded in PLGA nanofibers. In vitro biodegradation tests suggested that the bi-layered membrane possessed a proper degradation timeframe, which must function for at least 4 to 6 weeks. The cell experiments indicated that the bi-layered electrospun membrane possessed good cytocompatibility and proved the effective barrier potency of the small-sized pore layer. Furthermore, as revealed by the alkaline phosphate activity test, the PLGA/nHA layer possessed an improved osteogenic capacity for Human osteosarcoma cells (MG63). These results indicate that the bi-layered electrospun membrane may have potential for periodontal tissue regeneration. Graphical Abstract
引导组织再生膜(Guided tissue regeneration, GTR)不仅可以阻止不需要的组织向下生长到缺损处,还可以选择性地促进再生骨组织的生长,在牙周再生中起着至关重要的作用。本文通过调整静电纺丝参数,结合简易两步静电纺丝工艺,设计并制备了具有不同孔径的双层静电纺丝膜。小孔层(SL)由静电纺丝聚乳酸-羟基乙酸(PLGA)纳米纤维作为封闭层,而大孔导骨层(ML)是通过在静电纺丝过程中引入纳米羟基磷灰石(nHA)颗粒形成的。表面形貌、纳米纤维尺寸和孔径分布等形貌结果表明,纳米纤维具有致密的结构,孔径主要在4 ~ 7 μm之间。而ML结构松散,孔径主要在20 ~ 28 μm之间,有利于细胞的浸润。傅里叶变换红外光谱(FTIR)、能谱仪(EDS)和x射线衍射(XRD)结果表明,nHA颗粒均匀地负载在PLGA纳米纤维中。体外生物降解试验表明,双层膜具有适当的降解时间框架,其功能必须至少为4至6周。细胞实验表明,双层电纺丝膜具有良好的细胞相容性,证明了小孔层的有效屏障效能。此外,碱性磷酸盐活性试验显示,PLGA/nHA层对人骨肉瘤细胞(MG63)具有改善的成骨能力。这些结果表明双层电纺丝膜可能具有牙周组织再生的潜力。图形抽象
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引用次数: 0
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Journal of Bioactive and Compatible Polymers
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